Variant report
| Variant | rs7756228 |
|---|---|
| Chromosome Location | chr6:139985027-139985028 |
| allele | A/G |
| Outlinks | Ensembl UCSC |
- TF binding region (count:0)
- CpG islands (count:0)
- Chromatin interactive region (count:1)
- LncRNA region (count:0)
- Mature miRNA region (count: 0)
- miRNA target sites (count:0)
| No data |
| No data |
(count:1 , 50 per page) page:
1
| No. | Distal block | Cell Line | Cell type | Cell Stage |
|---|---|---|---|---|
| 1 | chr6:139694355..139696556-chr6:139984183..139986701,2 | MCF-7 | breast: |
| No data |
| No data |
| No data |
| Variant related genes | Relation type |
|---|---|
| ENSG00000164442 | Chromatin interaction |
rSNPs within LD-proxies of this variant (count:26)
| rs_ID | r2[population] |
|---|---|
| rs17053880 | 0.84[AFR][1000 genomes] |
| rs55689234 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs55755046 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs55961359 | 1.00[EUR][1000 genomes] |
| rs56245861 | 0.81[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs56335309 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs59731656 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs61478054 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs61657098 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs61693276 | 0.80[EUR][1000 genomes] |
| rs6905946 | 0.87[YRI][hapmap];0.84[AFR][1000 genomes] |
| rs6906246 | 1.00[CEU][hapmap];0.96[YRI][hapmap] |
| rs73556057 | 0.87[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs7739120 | 1.00[CHB][hapmap] |
| rs7743179 | 1.00[CEU][hapmap];0.96[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs7754093 | 0.93[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs9321747 | 0.87[YRI][hapmap] |
| rs9321749 | 0.86[YRI][hapmap];0.84[AFR][1000 genomes] |
| rs9376444 | 0.85[YRI][hapmap];0.84[AFR][1000 genomes] |
| rs9389706 | 0.87[YRI][hapmap];0.84[AFR][1000 genomes] |
| rs9389711 | 0.80[YRI][hapmap] |
| rs9403101 | 0.86[YRI][hapmap];0.84[AFR][1000 genomes] |
| rs9495558 | 0.82[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs9495560 | 1.00[CEU][hapmap];0.97[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
| rs9495561 | 0.86[YRI][hapmap];0.84[AFR][1000 genomes] |
| rs9495562 | 1.00[CEU][hapmap];0.97[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes] |
Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page:
1
| No. | Variant name | Chromosome position | Chromatin state | Related regulatory elements | Target genes | Extended variants | Associated traits |
|---|---|---|---|---|---|---|---|
| 1 | nsv869066 | chr6:139777114-140639695 | Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh | TF binding regionCpG islandChromatin interactive regionlncRNAmiRNA | 26 gene(s) | inside rSNPs | diseases |
| 2 | nsv516840 | chr6:139960833-140053704 | Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer | TF binding regionCpG islandChromatin interactive regionlncRNA | 2 gene(s) | inside rSNPs | diseases |
| No data |
Chromatin state (count:0 , 50 per page) page:
| No data |
